Canonical Allele Identifier: CA891844256

Gene: STK11

Linked Data

• ClinVar Variation Id: 574993
• ClinVar RCV Id: RCV000697074
• dbSNP Id: rs1568717471
• MyVariant Identifiers: chr19:g.1226599_1226600insTGAT (hg19) ; chr19:g.1226600_1226601insTGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226600_1226601insTGAT , CM000681.2:g.1226600_1226601insTGAT	GRCh38
NC_000019.9:g.1226599_1226600insTGAT , CM000681.1:g.1226599_1226600insTGAT	GRCh37
NC_000019.8:g.1177599_1177600insTGAT	NCBI36
NG_007460.2:g.42194_42195insTGAT , LRG_319:g.42194_42195insTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2856_*2857insTGAT	ENSP00000490268.2:n.*2856_*2857insTGAT
ENST00000585748.3:c.883_884insTGAT	ENSP00000477641.2:p.Ser295LeufsTer?
ENST00000585851.2:c.1081_1082insTGAT	ENSP00000467912.2:p.Ser361LeufsTer?
ENST00000326873.12:c.1255_1256insTGAT MANE Select	ENSP00000324856.6:p.Ser419LeufsTer?
ENST00000326873.11:c.1255_1256insTGAT	ENSP00000324856.6:p.Ser419LeufsTer?
ENST00000585465.2:n.2988_2989insTGAT
ENST00000586243.5:c.1254_1255-2insTGAT	ENSP00000467240.2:p.Ala419Ter
ENST00000589152.5:n.1953_1954insTGAT
NM_000455.4:c.1255_1256insTGAT , LRG_319t1:c.1255_1256insTGAT	NP_000446.1:p.Ser419LeufsTer?
XM_005259617.1:c.1250_1251insTGAT	XP_005259674.1:p.Arg418AspfsTer?
XM_011528209.1:c.1028_1029insTGAT	XP_011526511.1:p.Arg344AspfsTer?
XM_005259617.3:c.1250_1251insTGAT	XP_005259674.1:p.Arg418AspfsTer?
XM_011528209.2:c.1028_1029insTGAT	XP_011526511.1:p.Arg344AspfsTer?
XR_001753738.2:n.2061_2062insTGAT
XR_001753740.2:n.2031_2032insTGAT
NM_000455.5:c.1255_1256insTGAT MANE Select	NP_000446.1:p.Ser419LeufsTer?